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Esmolol added in repeated, cold, oxygenated blood cardioplegia improves myocardial function after cardiopulmonary bypass.
Dahle, Geir O; Salminen, Pirjo-Riitta; Moen, Christian A; Eliassen, Finn; Jonassen, Anne K; Haaverstad, Rune; Matre, Knut; Grong, Ketil.
Afiliação
  • Dahle GO; Section of Cardiothoracic Surgery, Department of Heart Disease, Haukeland University Hospital, Bergen, Norway; Department of Clinical Science. Electronic address: geir.olav.dahle@helse-bergen.no.
  • Salminen PR; Section of Cardiothoracic Surgery, Department of Heart Disease, Haukeland University Hospital, Bergen, Norway; Department of Clinical Science.
  • Moen CA; Department of Clinical Science.
  • Eliassen F; Section of Cardiothoracic Surgery, Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
  • Jonassen AK; Department of Biomedicine, University of Bergen, Bergen, Norway.
  • Haaverstad R; Section of Cardiothoracic Surgery, Department of Heart Disease, Haukeland University Hospital, Bergen, Norway; Department of Clinical Science.
  • Matre K; Department of Clinical Science.
  • Grong K; Department of Clinical Science.
J Cardiothorac Vasc Anesth ; 29(3): 684-93, 2015.
Article em En | MEDLINE | ID: mdl-25575405
ABSTRACT

OBJECTIVE:

This study investigated if the ß-receptor blocking agent esmolol, added to standard oxygenated blood cardioplegia, improved myocardial function after weaning from bypass.

DESIGN:

A block-randomized, blinded study.

SETTING:

A university laboratory.

PARTICIPANTS:

Twenty anesthetized pigs, Norwegian Landrace.

INTERVENTIONS:

After cardiopulmonary bypass, cardiac arrest was induced with cold (12°C), oxygenated blood cardioplegia, enriched with either esmolol or vehicle, repeated every 20 minutes. After 100 minutes the heart was reperfused and weaned. MEASUREMENTS AND MAIN

RESULTS:

Left ventricular function was evaluated with pressure-volume loops, local myocardial function with multilayer strain and strain rate by epicardial short-axis tissue Doppler imaging. One hour after declamping, preload recruitable stroke work did not differ between groups, but increased to 72±3 mmHg in esmolol-treated animals v 57±4 mmHg (p<0.001) in controls after 3 hours. Radial peak ejection strain rate also was increased by esmolol; 6.0±1.0 s(-1)v 2.9±0.3 s(-1) (p<0.001) in subendocardium and 3.9±0.5 s(-1)v 2.3±0.2 s(-1) (p<0.005) in the midmyocardium. Cardiac index was increased, 4.0±0.2 L/min/m(2) by esmolol v 3.3±0.1 L/min/m(2) for controls (p<0.05). Isovolumetric relaxation time constant was reduced by esmolol, 23±1 ms v 26±1 ms (p<0.025). Troponin-T did not differ and was 339±48 ng/L for the esmolol group and 357±55 ng/L for the control group (p = 0.81).

CONCLUSIONS:

Esmolol added to blood cardioplegia preserved systolic cardiac function during the first 3 hours after reperfusion in a porcine model with 100 minutes of cardioplegic arrest.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Propanolaminas / Ponte Cardiopulmonar / Temperatura Baixa / Antagonistas de Receptores Adrenérgicos beta 1 / Parada Cardíaca Induzida Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxigênio / Propanolaminas / Ponte Cardiopulmonar / Temperatura Baixa / Antagonistas de Receptores Adrenérgicos beta 1 / Parada Cardíaca Induzida Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article